Literature DB >> 22471789

Palladium-catalyzed cascade process to construct 1,2,5-trisubstituted pyrroles.

Yong-Qiang Zhang1, Dao-Yong Zhu, Bao-Sheng Li, Yong-Qiang Tu, Ji-Xin Liu, Yong Lu, Shao-Hua Wang.   

Abstract

A novel palladium-catalyzed cascade allylic amination/intramolecular hydroamination/isomerization process of protected enynol 1 and primary amine 2 has been explored, which constructs the important 1,2,5-trisubstituted pyrroles. This transformation offers an alternative synthetic methodology capable of generating substituted pyrroles in a straightforward way.
© 2012 American Chemical Society

Entities:  

Year:  2012        PMID: 22471789     DOI: 10.1021/jo300374v

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  An organocatalytic route to 2-heteroarylmethylene decorated N-arylpyrroles.

Authors:  Alexandre Jean; Jérôme Blanchet; Jacques Rouden; Jacques Maddaluno; Michaël De Paolis
Journal:  Beilstein J Org Chem       Date:  2013-07-24       Impact factor: 2.883

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.